TY  - JOUR
A1  - Guo, Ranran
A1  - Tian, Ye
A1  - Yang, Yueqi
A1  - Jiang, Qin
A1  - Wang, Yajun
A1  - Yang, Wuli
T1  - A Yolk-Shell nanoplatform for gene-silencing-enhanced photolytic ablation of cancer
JF  - Advanced functional materials
N2  - Noninvasive near-infrared (NIR) light responsive therapy is a promising cancer treatment modality; however, some inherent drawbacks of conventional phototherapy heavily restrict its application in clinic. Rather than producing heat or reactive oxygen species in conventional NIR treatment, here a multifunctional yolk-shell nanoplatform is proposed that is able to generate microbubbles to destruct cancer cells upon NIR laser irradiation. Besides, the therapeutic effect is highly improved through the coalition of small interfering RNA (siRNA), which is codelivered by the nanoplatform. In vitro experiments demonstrate that siRNA significantly inhibits expression of protective proteins and reduces the tolerance of cancer cells to bubble-induced environmental damage. In this way, higher cytotoxicity is achieved by utilizing the yolk-shell nanoparticles than treated with the same nanoparticles missing siRNA under NIR laser irradiation. After surface modification with polyethylene glycol and transferrin, the yolk-shell nanoparticles can target tumors selectively, as demonstrated from the photoacoustic and ultrasonic imaging in vivo. The yolk-shell nanoplatform shows outstanding tumor regression with minimal side effects under NIR laser irradiation. Therefore, the multifunctional nanoparticles that combining bubble-induced mechanical effect with RNA interference are expected to be an effective NIR light responsive oncotherapy.
KW  - cancer
KW  - gene silencing
KW  - near-infrared absorption
KW  - photolytic ablation
KW  - yolk-shell nanoparticles
Y1  - 2018
U6  - https://doi.org/10.1002/adfm.201706398
SN  - 1616-301X
SN  - 1616-3028
VL  - 28
IS  - 14
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Cook, Katherine V.
A1  - Li, Chuang
A1  - Cai, Haiyuan
A1  - Krumholz, Lee R.
A1  - Hambright, K. David
A1  - Paerl, Hans W.
A1  - Steffen, Morgan M.
A1  - Wilson, Alan E.
A1  - Burford, Michele A.
A1  - Grossart, Hans-Peter
A1  - Hamilton, David P.
A1  - Jiang, Helong
A1  - Sukenik, Assaf
A1  - Latour, Delphine
A1  - Meyer, Elisabeth I.
A1  - Padisak, Judit
A1  - Qin, Boqiang
A1  - Zamor, Richard M.
A1  - Zhu, Guangwei
T1  - The global Microcystis interactome
JF  - Limnology and oceanography
N2  - Bacteria play key roles in the function and diversity of aquatic systems, but aside from study of specific bloom systems, little is known about the diversity or biogeography of bacteria associated with harmful cyanobacterial blooms (cyanoHABs). CyanoHAB species are known to shape bacterial community composition and to rely on functions provided by the associated bacteria, leading to the hypothesized cyanoHAB interactome, a coevolved community of synergistic and interacting bacteria species, each necessary for the success of the others. Here, we surveyed the microbiome associated with Microcystis aeruginosa during blooms in 12 lakes spanning four continents as an initial test of the hypothesized Microcystis interactome. We predicted that microbiome composition and functional potential would be similar across blooms globally. Our results, as revealed by 16S rRNA sequence similarity, indicate that M. aeruginosa is cosmopolitan in lakes across a 280 degrees longitudinal and 90 degrees latitudinal gradient. The microbiome communities were represented by a wide range of operational taxonomic units and relative abundances. Highly abundant taxa were more related and shared across most sites and did not vary with geographic distance, thus, like Microcystis, revealing no evidence for dispersal limitation. High phylogenetic relatedness, both within and across lakes, indicates that microbiome bacteria with similar functional potential were associated with all blooms. While Microcystis and the microbiome bacteria shared many genes, whole-community metagenomic analysis revealed a suite of biochemical pathways that could be considered complementary. Our results demonstrate a high degree of similarity across global Microcystis blooms, thereby providing initial support for the hypothesized Microcystis interactome.
Y1  - 2019
U6  - https://doi.org/10.1002/lno.11361
SN  - 0024-3590
SN  - 1939-5590
VL  - 65
SP  - S194
EP  - S207
PB  - Wiley
CY  - Hoboken
ER  -